Nimenrix

Country: European Union

Language: Bulgarian

Source: EMA (European Medicines Agency)

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Active ingredient:

Neisseria meningitidis group A polysaccharide conjugated to tetanus toxoid, Neisseria meningitidis group C polysaccharide conjugated to tetanus toxoid, Neisseria meningitidis group W-135 polysaccharide conjugated to tetanus toxoid, Neisseria meningitidis group Y polysaccharide conjugated to tetanus toxoid

Available from:

Pfizer Europe MA EEIG

ATC code:

J07AH08

INN (International Name):

meningococcal groups A, C, W-135 and Y conjugate vaccine

Therapeutic group:

Ваксини

Therapeutic area:

Менингит, менингококов

Therapeutic indications:

Nimenrix е показан за активна имунизация на лица на възраст от 6 седмици срещу инвазивни менингококова болести, причинени от Neisseria менингит група A, C, W-135 и Y.

Product summary:

Revision: 36

Authorization status:

упълномощен

Authorization date:

2012-04-20

Patient Information leaflet

                                68
Б. ЛИСТОВКА
69
ЛИСТОВКА: ИНФОРМАЦИЯ ЗА ПОТРЕБИТЕЛЯ
NIMENRIX ПРАХ И РАЗТВОРИТЕЛ ЗА
ИНЖЕКЦИОНЕН РАЗТВОР В ПРЕДВАРИТЕЛНО
НАПЪЛНЕНА
СПРИНЦОВКА
Конюгатна ваксина срещу менингококи
от групи A, C, W-135 и Y
(Meningococcal groups A, C, W-135 and Y conjugate vaccine)
ПРОЧЕТЕТЕ ВНИМАТЕЛНО ЦЯЛАТА ЛИСТОВКА,
ПРЕДИ ДА ВИ БЪДЕ ПРИЛОЖЕНА ТАЗИ
ВАКСИНА, ТЪЙ
КАТО ТЯ СЪДЪРЖА ВАЖНА ЗА ВАС
ИНФОРМАЦИЯ.

Запазете тази листовка. Може да се
наложи да я прочетете отново.

Ако имате някакви допълнителни
въпроси, попитайте Вашия лекар или
фармацевт.

Тази ваксина е предписана на Вас или
на Вашето дете. Не я преотстъпвайте на
други
хора.

Ако получите някакви нежелани
лекарствени реакции, уведомете Вашия
лекар или
фармацевт. Това включва и всички
възможни нежелани реакции, неописани
в тази
листовка. Вижте точка 4.
Тази листовка е написана, като се
приема, че лицето, на което се прилага
ваксината ще я
прочете, но ваксината може да бъде
приложена както на възрастни, така и
на деца, и Вие може
да я прочетете заради Вашето дете.
КАКВО СЪДЪРЖА ТАЗИ ЛИСТОВКА
1.
Какво представлява Nimenrix и за какво се
използва
2.
Какво трябва да знаете, преди да Ви
бъде приложен Nimenrix
3.
Как се прил
                                
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Summary of Product characteristics

                                1
ПРИЛОЖЕНИЕ I
КРАТКА ХАРАКТЕРИСТИКА НА ПРОДУКТА
2
1.
ИМЕ НА ЛЕКАРСТВЕНИЯ ПРОДУКТ
Nimenrix прах и разтворител за
инжекционен разтвор в предварително
напълнена спринцовка
Конюгатна ваксина срещу менингококи
от групи A, C, W-135 и Y
(Meningococcal groups A, C, W-135 and Y conjugate vaccine)
2.
КАЧЕСТВЕН И КОЛИЧЕСТВЕН СЪСТАВ
След разтваряне една доза (0,5 ml) от
ваксината съдържа:
_Neisseria meningitidis_ полизахарид група A
1
(_Neisseria meningitidis_ group A polysaccharide
1
)
5 микрограма
_Neisseria meningitidis _полизахарид група C
1
(_Neisseria meningitidis_ group C polysaccharide
1
)
5 микрограма
_Neisseria meningitidis_ полизахарид група W-135
1
(_Neisseria meningitidis_ group W-135 polysaccharide
1
)
5 микрограма
_Neisseria meningitidis_ полизахарид група Y
1
(_Neisseria meningitidis_ group Y polysaccharide
1
)
5 микрограма
1
конюгиран с тетаничен токсоид
(протеинов носител)
44 микрограма
За пълния списък на помощните
вещества вижте точка 6.1.
3.
ЛЕКАРСТВЕНА ФОРМА
Прах и разтворител за инжекционен
разтвор
Прахът или компактната маса са бели.
Разтворителят е прозрачен и
безцветен.
4.
КЛИНИЧНИ ДАННИ
4.1
ТЕРАПЕВТИЧНИ ПОКАЗАНИЯ
Nimenrix е показан за активна имунизация
срещу инвазивно менингококово
заболяване,
причинявано от _Neisseria meningitidis_ групи A, C,
W-135 и Y, при лица на възраст от 6 седмици.
4.2
ДОЗИРОВКА И
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Spanish 25-05-2022
Public Assessment Report Public Assessment Report Spanish 26-08-2019
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Public Assessment Report Public Assessment Report Czech 26-08-2019
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Public Assessment Report Public Assessment Report Danish 26-08-2019
Patient Information leaflet Patient Information leaflet German 25-05-2022
Public Assessment Report Public Assessment Report German 26-08-2019
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Public Assessment Report Public Assessment Report Estonian 26-08-2019
Patient Information leaflet Patient Information leaflet Greek 25-05-2022
Public Assessment Report Public Assessment Report Greek 26-08-2019
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Public Assessment Report Public Assessment Report English 26-08-2019
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Public Assessment Report Public Assessment Report French 26-08-2019
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Public Assessment Report Public Assessment Report Italian 26-08-2019
Patient Information leaflet Patient Information leaflet Latvian 25-05-2022
Public Assessment Report Public Assessment Report Latvian 26-08-2019
Patient Information leaflet Patient Information leaflet Lithuanian 25-05-2022
Summary of Product characteristics Summary of Product characteristics Lithuanian 25-05-2022
Public Assessment Report Public Assessment Report Lithuanian 26-08-2019
Patient Information leaflet Patient Information leaflet Hungarian 25-05-2022
Summary of Product characteristics Summary of Product characteristics Hungarian 25-05-2022
Public Assessment Report Public Assessment Report Hungarian 26-08-2019
Patient Information leaflet Patient Information leaflet Maltese 25-05-2022
Public Assessment Report Public Assessment Report Maltese 26-08-2019
Patient Information leaflet Patient Information leaflet Dutch 25-05-2022
Public Assessment Report Public Assessment Report Dutch 26-08-2019
Patient Information leaflet Patient Information leaflet Polish 25-05-2022
Public Assessment Report Public Assessment Report Polish 26-08-2019
Patient Information leaflet Patient Information leaflet Portuguese 25-05-2022
Summary of Product characteristics Summary of Product characteristics Portuguese 25-05-2022
Public Assessment Report Public Assessment Report Portuguese 26-08-2019
Patient Information leaflet Patient Information leaflet Romanian 25-05-2022
Public Assessment Report Public Assessment Report Romanian 26-08-2019
Patient Information leaflet Patient Information leaflet Slovak 25-05-2022
Public Assessment Report Public Assessment Report Slovak 26-08-2019
Patient Information leaflet Patient Information leaflet Slovenian 25-05-2022
Summary of Product characteristics Summary of Product characteristics Slovenian 25-05-2022
Public Assessment Report Public Assessment Report Slovenian 26-08-2019
Patient Information leaflet Patient Information leaflet Finnish 25-05-2022
Public Assessment Report Public Assessment Report Finnish 26-08-2019
Patient Information leaflet Patient Information leaflet Swedish 25-05-2022
Public Assessment Report Public Assessment Report Swedish 26-08-2019
Patient Information leaflet Patient Information leaflet Norwegian 25-05-2022
Summary of Product characteristics Summary of Product characteristics Norwegian 25-05-2022
Patient Information leaflet Patient Information leaflet Icelandic 25-05-2022
Summary of Product characteristics Summary of Product characteristics Icelandic 25-05-2022
Patient Information leaflet Patient Information leaflet Croatian 25-05-2022
Public Assessment Report Public Assessment Report Croatian 26-08-2019

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